Johnson & Johnson
Regulatory Affairs Associate
Regulatory Affairs Associate
1 year contract, potential to renew
Come and join us!
Do you wish to work in a world-class organization trying your hands at something you have dreamt of doing?
“FIND YOUR PLACE” by joining our client Johnson & Johnson
Get an opportunity to explore new technology, learn new skills, enjoy the diverse and open culture, engagement and care, flexible working model, career opportunities, competitive salary and bonus, and endless amenities and benefits.
Johnson & Johnson Worksense Singapore (via Randstad Sourceright) is responsible for finding, engaging, and contracting talent for the Johnson & Johnson contingent workforce.
About Johnson & Johnson
At Johnson & Johnson, they believe health is everything. As a focused healthcare company, with expertise in Innovative Medicine and MedTech, they are empowered to tackle the world’s toughest health challenges, innovate through science and technology, and transform patient care.
As an equal opportunity employer Johnson & Johnson value diversity at their company. They don’t discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Job Description
The Regulatory Affairs Associate is a member of ASPAC Special Project. He or she is responsible for actively contributing to the regulatory compliance of medical devices. He or she is also responsible for data integrity and maintenance across multiple regulatory systems utilized by J&J.
This position reports to the Special Project RA lead (SEA cluster).
Responsibilities
1. The Regulatory Affairs Associate main responsibility is to support the ASPAC markets on MedTech regulatory affairs matters.
2. Creation and maintenance of regulatory information in Regulatory Database system.
3. Creation of routine reports to ASPAC markets related to regulatory compliance matters (submission schedules, eligibility and etc.).
4. Creation of routine monthly Performance metrics report to ASPAC markets using basic IT skills
5. Extended roles in providing administrative support to local Singapore Regulatory Affairs MedTech department, including RA database update, data analysis and local database maintenance.
Requirements
· A minimum Bachelor’s degree in any Business or Science Field
· Good at Power BI, MS Word, MS Excel, MS Power Point
· Has a strong sense of responsibility on meeting due/target and quality/integrity/accuracy of the output
· The incumbent must have the ability to work effectively without supervision and process requests/work within required timeframes.
· Strives to acquire a deeper understanding of medical and scientific and technological developments.
· Views new and ambiguous challenges as a learning opportunity
· Leadership Competencies:
Assists and supports others in interactions with team members and internal stakeholders by partnering and collaborating with them effectively.
Interested parties, please apply through this link https://jnj-apac.talent-pool.com/projects OR click on APPLY button.
Alternatively, you can share your CV at joleyn.chin@randstadsourceright.com.sg
EA License: 94C3609
Reg No: R1440247